Observation Study: Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients
Superselective Drug-Eluting Chemoembolization in Unresectable Intermediate and Advanced HCC Patients: Safety & Efficacy Registry in Taiwan (SUPER- Taiwan)
調査の概要
状態
条件
詳細な説明
The purpose of this multicenter registry is to gather the safety, efficacy and survival data in intermediate and advanced HCC patients treated drug-eluting microsphere in Taiwan in order to provide clinical evidence on deTACE in HCC management to physicians in the region, and to support the application of in treating advanced HCC patients.
Primary Objective:
To collect 1-year overall survival of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients in Taiwan.
Secondary Objectives:
- To evaluate the overall tumor response of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients. The tumor response is according to Modified Response Evaluation Criteria in Solid Tumors (mRECIST) criteria.
- To evaluate the local tumor response (in the tumor(s) treated with drug-eluting microsphere) by chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
- To evaluate the safety profile of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
Exploratory Objectives:
- To evaluate the downstaging and downsizing potential of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients to within Milan Criteria and to within Resection margin.
- To collect time-to-progression (TTP) and progress-free-survival (PFS) data of chemoembolization with drug-eluting microsphere in intermediate and advanced HCC patients.
研究の種類
入学 (予想される)
連絡先と場所
研究場所
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Taipei、台湾、11217
- 募集
- Taipei Veterans General Hospital
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
サンプリング方法
調査対象母集団
説明
Inclusion Criteria:Patients must meet all of the following inclusion criteria in order to be entered into the study:
- Age 20 or older.
- Patient has signed informed consent.
Patient must have a diagnosis of hepatocellular cancer confirmed by AASLD and at least one of the following method:
- Magnetic resonance imaging (MRI) with early enhancement and delayed enhancement washout of at least one solid liver lesion > 1 cm.
- Contrast enhanced computed tomography (CT) with early enhancement and delayed enhancement washout of at least one solid liver lesion > 1 cm.
- Histological confirmation is required for lesions with inconclusive features.
Patient must not be suitable for treatment by resection or percutaneous ablation at time of study entry.
- Patients not suitable for ablation due to lesion location may be enrolled.
- Patients with HCC recurrence but not suitable for resection or ablation maybe enrolled.
Patient MUST be with either BCLC stage B OR C, and meet the following criteria:
- Stage Child-Pugh A or B AND
- Performance status ECOG ≤ 1 WITH Vascular Invasion or WITHOUT Vascular invasion.
- Patient has a life expectancy of at least 6 months.
Exclusion Criteria:If patients meet any of the following criteria they may not be entered into the study:
- Current or previous treatment with chemo- or radiation therapy or sorafenib or drug-eluting chemoembolization (deTACE).
- Patients with concurrent cancer except non-melanomatous skin cancer.
- Female patients who are pregnant, breastfeeding, or premenopausal and not using an effective method of contraceptive.
- Performance status ECOG > 1.
- Child-Pugh Class C.
- Occlusive tumor thrombus to the main portal trunk.
- Active gastrointestinal bleeding.
- Evidence of uncorrectable bleeding diathesis.
- Extra-Hepatic spread of the HCC.
- Encephalopathy not adequately controlled medically.
- Presence of ascites not controlled medically.
- Any contraindication for MRI/ CT (eg. metallic implants).
- Allergy to contrast media that cannot be managed with prophylaxis.
- Any contraindication to arteriography.
- Any contraindication for doxorubicin administration.
- Any contraindication for hepatic embolization. Porto-systemic shunt, or an arteriovenous shunt that cannot be adequately closed prior to chemoembolization. Hepatofugal blood flow. Serum creatinine > 2mg/dL. Other condition deemed exclusionary by physician. Uncorrectable impaired clotting.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 観測モデル:ケースのみ
- 時間の展望:見込みのある
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Overall survival
時間枠:1 year
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To define all participants from the day of the first HepaSphere Treatment until end of study or death is reported, whichever comes first.
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1 year
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二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Tumor Response
時間枠:1 year
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Tumor response will be assessed using modified Response Evaluation Criteria In Solid Tumors (mRECIST) criteria to evaluate tumor necrosis under CT/ MRI and will be presented as %.
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1 year
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Adverse Event (AE)
時間枠:1 year
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Adverse event will be accessed according to CTCAE 4.0 after treatments until end of study or death.
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1 year
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その他の成果指標
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
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Exploratory Objectives, Time-To-Progression (TTP)
時間枠:1 year
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To define all participants from the day of the first HepaSphere Treatment until tumor progression or death is first reported, whichever comes first.
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1 year
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Exploratory Objectives, Downstaging
時間枠:1 year
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Tumor staging will be accessed according to BCLC staging system and Milan criteria, and will be reviewed at follow-up until end of study or death.
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1 year
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協力者と研究者
協力者
捜査官
- 主任研究者:Yi-Hsiang Huang, M.D. Ph.D.、Taipei Veterans General Hospital, Taiwan
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (予想される)
研究の完了 (予想される)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。
肝細胞癌の臨床試験
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